PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
Use this interactive explorer to filter all results across submission entries and multiple dimensions.
| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
32651-32700 / 86044 show all | |||||||||||||||
| ckim-dragen | INDEL | * | map_l125_m2_e1 | het | 95.7012 | 96.4489 | 94.9650 | 90.2767 | 1358 | 50 | 1358 | 72 | 8 | 11.1111 | |
| ckim-dragen | INDEL | D16_PLUS | map_l100_m0_e0 | het | 74.6228 | 89.4737 | 64.0000 | 97.0449 | 17 | 2 | 16 | 9 | 1 | 11.1111 | |
| ckim-dragen | INDEL | D16_PLUS | map_l100_m1_e0 | het | 80.0532 | 93.4783 | 70.0000 | 96.1710 | 43 | 3 | 42 | 18 | 2 | 11.1111 | |
| gduggal-snapplat | INDEL | D6_15 | map_l100_m1_e0 | * | 38.7543 | 25.1938 | 83.9286 | 94.2915 | 65 | 193 | 47 | 9 | 1 | 11.1111 | |
| gduggal-snapplat | INDEL | D6_15 | map_l100_m1_e0 | het | 43.8202 | 30.9524 | 75.0000 | 93.9394 | 39 | 87 | 27 | 9 | 1 | 11.1111 | |
| gduggal-snapfb | INDEL | D1_5 | map_l100_m1_e0 | het | 95.6711 | 96.4433 | 94.9111 | 81.1539 | 1166 | 43 | 1175 | 63 | 7 | 11.1111 | |
| gduggal-snapfb | INDEL | I1_5 | map_l125_m1_e0 | het | 95.1089 | 95.6790 | 94.5455 | 85.1619 | 465 | 21 | 468 | 27 | 3 | 11.1111 | |
| gduggal-snapfb | INDEL | I1_5 | map_l125_m2_e0 | het | 95.2161 | 95.7746 | 94.6640 | 86.7331 | 476 | 21 | 479 | 27 | 3 | 11.1111 | |
| gduggal-snapfb | INDEL | I1_5 | map_l125_m2_e1 | het | 95.3187 | 95.8661 | 94.7776 | 86.8347 | 487 | 21 | 490 | 27 | 3 | 11.1111 | |
| gduggal-snapvard | SNP | tv | tech_badpromoters | * | 85.8248 | 84.7222 | 86.9565 | 55.7692 | 61 | 11 | 60 | 9 | 1 | 11.1111 | |
| gduggal-snapvard | SNP | tv | tech_badpromoters | het | 80.0000 | 84.8485 | 75.6757 | 60.6383 | 28 | 5 | 28 | 9 | 1 | 11.1111 | |
| hfeng-pmm1 | INDEL | * | map_l125_m0_e0 | het | 96.8885 | 95.4003 | 98.4238 | 87.4146 | 560 | 27 | 562 | 9 | 1 | 11.1111 | |
| gduggal-snapvard | INDEL | C1_5 | map_l100_m1_e0 | * | 0.0000 | 0.0000 | 49.0566 | 95.2861 | 0 | 0 | 78 | 81 | 9 | 11.1111 | |
| gduggal-snapvard | INDEL | C6_15 | map_siren | * | 0.0000 | 0.0000 | 52.6316 | 96.6841 | 0 | 0 | 10 | 9 | 1 | 11.1111 | |
| gduggal-snapvard | INDEL | C6_15 | map_siren | het | 0.0000 | 0.0000 | 50.0000 | 96.4637 | 0 | 0 | 9 | 9 | 1 | 11.1111 | |
| jmaeng-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.8006 | 99.8255 | 99.7757 | 49.8187 | 4004 | 7 | 4004 | 9 | 1 | 11.1111 | |
| jmaeng-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.7054 | 99.7642 | 99.6466 | 52.8246 | 2538 | 6 | 2538 | 9 | 1 | 11.1111 | |
| ltrigg-rtg2 | INDEL | * | map_l125_m0_e0 | * | 96.7585 | 94.6712 | 98.9399 | 82.0279 | 835 | 47 | 840 | 9 | 1 | 11.1111 | |
| ltrigg-rtg1 | INDEL | * | map_l100_m2_e0 | het | 96.7120 | 94.3650 | 99.1788 | 77.1166 | 2177 | 130 | 2174 | 18 | 2 | 11.1111 | |
| hfeng-pmm3 | SNP | ti | map_l150_m1_e0 | het | 99.3161 | 99.2158 | 99.4166 | 75.5923 | 12273 | 97 | 12269 | 72 | 8 | 11.1111 | |
| hfeng-pmm3 | INDEL | D16_PLUS | map_siren | * | 92.9353 | 92.3077 | 93.5714 | 92.9895 | 132 | 11 | 131 | 9 | 1 | 11.1111 | |
| jlack-gatk | INDEL | D6_15 | map_l150_m2_e1 | * | 93.1818 | 96.4706 | 90.1099 | 93.5825 | 82 | 3 | 82 | 9 | 1 | 11.1111 | |
| jlack-gatk | INDEL | I6_15 | segdup | * | 95.7507 | 96.5714 | 94.9438 | 93.8621 | 169 | 6 | 169 | 9 | 1 | 11.1111 | |
| hfeng-pmm2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.8596 | 98.1676 | 99.5615 | 75.0651 | 14304 | 267 | 14304 | 63 | 7 | 11.1111 | |
| hfeng-pmm2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.8596 | 98.1676 | 99.5615 | 75.0651 | 14304 | 267 | 14304 | 63 | 7 | 11.1111 | |
| hfeng-pmm1 | INDEL | D16_PLUS | map_siren | het | 92.3788 | 96.1538 | 88.8889 | 94.1727 | 75 | 3 | 72 | 9 | 1 | 11.1111 | |
| mlin-fermikit | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 94.6799 | 92.3387 | 97.1429 | 70.2456 | 916 | 76 | 918 | 27 | 3 | 11.1111 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.3986 | 97.4766 | 99.3382 | 61.3636 | 1352 | 35 | 1351 | 9 | 1 | 11.1111 | |
| ltrigg-rtg2 | SNP | * | map_l125_m1_e0 | het | 98.5086 | 97.2457 | 99.8048 | 55.1586 | 27610 | 782 | 27610 | 54 | 6 | 11.1111 | |
| ltrigg-rtg2 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 91.3928 | 87.7828 | 95.3125 | 88.4128 | 194 | 27 | 183 | 9 | 1 | 11.1111 | |
| ltrigg-rtg2 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 90.6003 | 88.1579 | 93.1818 | 89.0638 | 134 | 18 | 123 | 9 | 1 | 11.1111 | |
| ltrigg-rtg2 | SNP | tv | map_l150_m1_e0 | * | 98.6367 | 97.4707 | 99.8310 | 62.1132 | 10636 | 276 | 10635 | 18 | 2 | 11.1111 | |
| mlin-fermikit | INDEL | D16_PLUS | map_l125_m0_e0 | * | 42.1053 | 66.6667 | 30.7692 | 92.3754 | 8 | 4 | 8 | 18 | 2 | 11.1111 | |
| mlin-fermikit | INDEL | D16_PLUS | map_l125_m2_e1 | * | 55.2632 | 75.0000 | 43.7500 | 93.7662 | 21 | 7 | 21 | 27 | 3 | 11.1111 | |
| qzeng-custom | INDEL | D6_15 | map_l125_m0_e0 | het | 78.9744 | 75.8621 | 82.3529 | 94.6875 | 22 | 7 | 42 | 9 | 1 | 11.1111 | |
| qzeng-custom | SNP | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 80.0000 | 80.9524 | 79.0698 | 97.5058 | 34 | 8 | 34 | 9 | 1 | 11.1111 | |
| qzeng-custom | SNP | * | lowcmp_SimpleRepeat_diTR_51to200 | het | 71.4286 | 74.0741 | 68.9655 | 97.9374 | 20 | 7 | 20 | 9 | 1 | 11.1111 | |
| raldana-dualsentieon | INDEL | * | map_l125_m1_e0 | het | 97.3655 | 96.7790 | 97.9592 | 85.1598 | 1292 | 43 | 1296 | 27 | 3 | 11.1111 | |
| raldana-dualsentieon | INDEL | * | map_l125_m2_e0 | het | 97.3979 | 96.7649 | 98.0392 | 86.1441 | 1346 | 45 | 1350 | 27 | 3 | 11.1111 | |
| raldana-dualsentieon | INDEL | * | map_l125_m2_e1 | het | 97.4295 | 96.8040 | 98.0631 | 86.2674 | 1363 | 45 | 1367 | 27 | 3 | 11.1111 | |
| raldana-dualsentieon | INDEL | * | map_l150_m0_e0 | * | 96.6054 | 96.6926 | 96.5184 | 90.3545 | 497 | 17 | 499 | 18 | 2 | 11.1111 | |
| qzeng-custom | INDEL | D6_15 | func_cds | * | 85.9267 | 90.6977 | 81.6327 | 50.0000 | 39 | 4 | 40 | 9 | 1 | 11.1111 | |
| raldana-dualsentieon | SNP | tv | map_l250_m0_e0 | * | 97.1091 | 96.6013 | 97.6222 | 91.9886 | 739 | 26 | 739 | 18 | 2 | 11.1111 | |
| raldana-dualsentieon | SNP | tv | segdup | * | 99.5671 | 99.7656 | 99.3693 | 91.0002 | 8512 | 20 | 8508 | 54 | 6 | 11.1111 | |
| bgallagher-sentieon | SNP | ti | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.8465 | 99.9232 | 99.7699 | 29.4425 | 3903 | 3 | 3902 | 9 | 1 | 11.1111 | |
| cchapple-custom | INDEL | * | map_l250_m1_e0 | * | 93.3027 | 95.0820 | 91.5888 | 95.3992 | 290 | 15 | 294 | 27 | 3 | 11.1111 | |
| anovak-vg | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 8.0635 | 4.5113 | 37.9310 | 60.2740 | 6 | 127 | 22 | 36 | 4 | 11.1111 | |
| asubramanian-gatk | INDEL | D16_PLUS | map_siren | * | 92.1758 | 90.9091 | 93.4783 | 95.3892 | 130 | 13 | 129 | 9 | 1 | 11.1111 | |
| asubramanian-gatk | SNP | tv | segdup | * | 97.9981 | 96.6831 | 99.3493 | 93.1884 | 8249 | 283 | 8245 | 54 | 6 | 11.1111 | |
| asubramanian-gatk | INDEL | D1_5 | segdup | * | 98.9561 | 98.7307 | 99.1826 | 95.3977 | 1089 | 14 | 1092 | 9 | 1 | 11.1111 | |